ladd syndrome Gene Set

Dataset OMIM Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An autosomal dominant disease that is characterized by abnormalities affecting the lacrimal and salivary glands and ducts, ears, teeth and fingers and toes. (Human Disease Ontology, DOID_0050331)
External Link http://www.omim.org/entry/149730
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Genes

3 genes associated with the ladd syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

Symbol Name
FGF10 fibroblast growth factor 10
FGFR2 fibroblast growth factor receptor 2
FGFR3 fibroblast growth factor receptor 3